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  1. 1421

    The Hereditary Hyperferritinemia-Cataract Syndrome in 2 Italian Families by Katia Perruccio, Francesco Arcioni, Carla Cerri, Roberta La Starza, Donatella Romanelli, Ilaria Capolsini, Maurizio Caniglia

    Published 2013-01-01
    “…Both displayed heterozygosity for C33T mutation in the ferritin light chain iron response element. A 7-year-old boy from another family was referred to our unit because of hyperferritinemia. …”
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  2. 1422

    Case report: Toxic epidermal necrolysis as a unique presentation of acute graft versus host disease in a pediatric patient by Elizabeth Marlowe, Rachel Palmer, April L. Rahrig, Devin Dinora, Jessica Harrison, Jodi Skiles, Mahvish Q. Rahim

    Published 2025-01-01
    “…Management and outcomes of pediatric patients with this overlapping, severe presentation have rarely been described.Case presentationThis report describes an 11-year-old boy with refractory T-cell acute lymphoblastic leukemia who received peripheral blood SCT from a matched unrelated donor. …”
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  3. 1423

    Case Report: Clinical awareness about the effect of laser interstitial thermal therapy on pediatric high-grade brain tumors after radiotherapy by Sandra Fernandes Dias, Markus F. Oertel, Ana Guerreiro Stücklin, Nicolas U. Gerber, Elisa Colombo, Tristan P. C. van Doormaal, Niklaus Krayenbühl

    Published 2025-01-01
    “…The first case was an 11-year-old boy with a periventricular metastasis of a recurrent anaplastic ependymoma treated with proton-therapy and radiosurgery. …”
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  4. 1424

    Autoimmune Complications after Hematopoietic Stem Cell Transplantation in Children with Nonmalignant Disorders by Abdalla Khalil, Irena Zaidman, Reuven Bergman, Ronit Elhasid, Myriam Weyl Ben-Arush

    Published 2014-01-01
    “…Five (5.4%) patients were diagnosed with scleroderma manifestations, six (6.5%) with vitiligo, six (6.5%) with autoimmune hemolytic anemia (AIHA), six (6.5%) with idiopathic thrombocytopenia, three (3.3%) with mild leucopenia, two (2.2%) with aplastic anemia, two (2.2%) (one boy, one girl) with autoimmune thyroid disease, and one (1.1%) with autoimmune hepatitis. …”
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  5. 1425

    Acute fatty liver of pregnancy: An atypical case report by Riska Subono, Nurul Hikmah

    Published 2024-11-01
    “…This patient was diagnosed with AFLP based on Swansea Criteria (7 out of 10) and terminated pregnancy two days after diagnosis. A baby boy was born with birth weight 1.100 gr, birth length 34 cm, apgar score (AS) 9 and 10 at 1 and 5 minutes. …”
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  6. 1426
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  9. 1429

    Isoflurane Induced Malignant Hyperthermia in a Patient with Glucose 6-Phosphate Dehydrogenase Deficiency and Growth Hormone Abuse by Hojatolah Ravaei, Mohammad Javad Yavari Barhaghtalab, Vahid Salehi, Hossein Hejr

    Published 2020-01-01
    “…Our patient was a 17-year-old boy with right lower quadrant abdominal pain and tenderness who underwent appendectomy. …”
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  10. 1430

    Overlooking the Obvious during the COVID-19 Pandemic: Dyspnoea with Asymmetric Breath Sounds in a Toddler by Heli Salmi, Heini Harve-Rytsälä, Paula Rautiainen, Sari Pyörälä, Johanna Hästbacka

    Published 2021-01-01
    “…The patient was a 20-month-old healthy boy. In the morning, he had coughed while drinking milk. …”
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  11. 1431

    Le continent noir du désir masculin : Colet et Flaubert, encore by Barbara Vinken

    Published 2010-09-01
    “…The slippers, a most classic fetish, by a metonymic displacement take the place of the maternal phallus, whose absence is discovered with horror. This lack makes the boy realize the possibility of castration. The fetish object is both memory of and triumph over castration. …”
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  12. 1432

    Aspirasi Benda Asing Paku dengan Komplikasi Atelektasis Paru dan Aspirasi Benda Asing Jarum Pentul Tanpa Komplikasi by Novialdi ., Fachzi Fitri, Histawara Subroto

    Published 2015-05-01
    “…Bronchoscopy is the management  for aspirated sharp foreign body extraction   Reported two cases of a sharp foreign body aspiration is a boy, aged 6 year old with nail aspiration complication with<br />lung atelectasis and a girl, aged 14 year old with aspirations of a pin without complications that have been successfully <br />extract  using rigid bronchoscopy . …”
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  13. 1433
  14. 1434

    Resolution of unilateral sensorineural hearing loss in a pediatric patient with a severe phenotype of Muckle-Wells syndrome treated with Anakinra: a case report and review of the l... by Cinzia Marchica, Faisal Zawawi, Dania Basodan, Rosie Scuccimarri, Sam J. Daniel

    Published 2018-01-01
    “…Case presentation A 3-year-old boy was referred to our hospital to assess for the possibility of MWS given a history of hives and recurrent episodes of fever with a family history of MWS in his mother. …”
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  15. 1435

    A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication with Autism Spectrum Disorder and Dyskinesia by Luna Bajracharya, Meena Lall, Sunita Bijarnia-Mahay, Praveen Kumar, Imran Mushtaq, Pushpa Saviour, Preeti Paliwal, Anju Joshi, Shruti Agarwal, Praveen Suman

    Published 2023-01-01
    “…A 3 years and 11 months old boy with global developmental delay had repetitive behaviors and hyperkinetic movements. …”
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  16. 1436

    Erol Güngör’ün İslam’a Dair Sosyolojik Mülahazaları by İslam Can

    Published 2016-08-01
    “…Güngör, halkçılığı temele aldığı bir milliyetçilik anlayışı geliştirmesi, İslam’ın ve İslam ülkelerinin problemlerine çözüm üretmedeki gönüllülüğü, İslam’ın yeniden diri bir medeniyet geliştirerek tarih sahnesinde boy göstermesi gerektiğini ifade eden düşünceleriyle, bugün dahi eksikliği hissedilen bir mütefekkirdir. …”
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  17. 1437

    Combined negative pressure wound therapy with new wound dressings to repair a ruptured giant omphalocele in a neonate: a case report and literature review by Shulin Hou, Zeyao Shi, Xiaowen Li, Ru Yang, Yan Song, Zhaolan Zeng

    Published 2025-01-01
    “…Case presentation The patient was a baby boy aged 2 days, weighing 2930 g. He was diagnosed with a giant omphalocele with a partial intestine exposed. …”
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  18. 1438

    DEVIATION AND ATROPHY OF MIDDLE PHALANX OF HAND FOLLOWING PARTIAL SEPARATION IN SYNDACTYLY PATIENT: THEIR FAULT OR OURS? by Diana Murtiati Kusuma, Iswinarno Doso Saputro, Sitti Rizaliyana, Beta Subakti Nata’atmadja

    Published 2018-06-01
    “…Case Illustration: A 13-year old boy, presented with fusion of all fingers of the right hand at birth. …”
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  19. 1439
  20. 1440

    Risdiplam utilization, adherence, and associated health care costs for patients with spinal muscular atrophy: a United States retrospective claims database analysis by Anish Patel, Walter Toro, Min Yang, Wei Song, Raj Desai, Mingchen Ye, Nadia Tabatabaeepour, Omar Dabbous

    Published 2024-12-01
    “…One patient had SMA type 1 (a 1-year-old boy), 18 had type 2 (mean ± SD age: 7.9 ± 5.7 years; 61% female), 47 had type 3 (17.3 ± 10.2 years; 55% female), and 20 had type 4 (38.2 ± 11.6 years; 55% female). …”
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